Abstract
Objective
To investigate the possible effect of unphysiologically low pH in dialysis fluid on peritoneal transport.
Design
A 4-hour single-cycle experimental session of peritoneal dialysis was performed in six 5prague-Dawley rats using Dianeal 3.86% solution modified by adding 5 mmol/L of sodium hydroxide, neutral pH solution (NpH5) (pH 7.4). The intraperitoneal volume (V D) and peritoneal bulkfluid reabsorption (aa) were calculated using a marker, 1311–labeled human serum albumin (RI5A). The diffusive mass transport coefficient (KBD) as well as sieving coefficient (5) for glucose, urea, sodium, and potassium were calculated using the Babb-Randerson-Farrell model. The same study was performed in seven rats using Dianeal 3.86% solution, acidic pH solution (ApH5) (pH 5.7) to provide control values.
Results
The dialysate pH was stable with NpH5; 45 min after the infusion of ApH5 it increased rapidly and reached the physiological value 7.4. Dialysate volume and KBD values for sodium and potassium with NpH5 were significantly higher than with ApH5, while the KBD values for glucose and urea did not differ between the two solutions. 5 values for sodium and urea did not differ between the two solutions, while the values for glucose and potassium with NpH5 were significantly higher and lower, respectively, than the values with ApH5 (0.92±1.04 vs 0.04±0.63 and 0.56±060 vs 1.15±0.39, p < 0.05). The absorption of glucose from the dialysis solution expressed as a percentage of the initial amount of dialysate glucose was significantly lower with NpH5 than with ApH5 at 30 min (17.3±1.7% vs 29.7±2.0%, p < 0.05).
Conclusion
We conclude that the peritoneal transport of fluid and small solutes might to some extent be influenced by the acidity of the dialysis solution. The vasodilatory effect of acidic dialysis solution might be the most important mechanism for these differences. However, a larger KBD value and a lower 5 value for potassium and higher 5 values for glucose during dialysis with the neutral dialysis solution may indicate that transport mechanisms other than simple passive transport are involved in peritoneal transport for glucose and electrolytes.
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